Bromide

Bromide

SCHEMBL5550573

C=CC[N+](C)(CC=C)CCCCCCCCCC[N+](C)(CC=C)CC=C.[Br-].[Br-]

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 3/20 0.41
MEN1 O00255 4/20 0.41
KMT2A Q03164 4/20 0.41
APEX1 P27695 3/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
KDM4E B2RXH2 2/20 0.41
PMP22 Q01453 2/20 0.41
LMNA P02545 2/20 0.39
NFKB1 P19838 2/20 0.36
HSD17B10 Q99714 2/20 0.36
TSHR P16473 2/20 0.36
HRH3 Q9Y5N1 1/20 0.36
RAB9A P51151 1/20 0.36
BBOX1 O75936 1/20 0.36
NPSR1 Q6W5P4 1/20 0.35
DNM1 Q05193 7/20 0.35
HSP90AA1 P07900 1/20 0.32
RAD52 P43351 1/20 0.32
ALDH1A1 P00352 1/20 0.32
TP53 P04637 1/20 0.32

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Bromide SCHEMBL5551175 1.00 MEN1 (0.41) MEN1KMT2AAPEX1SMN1; SMN2ACHE
SCHEMBL5550564 0.97 KMT2A (0.38) MEN1KMT2AAPEX1SMN1; SMN2ACHE
SCHEMBL13779370 0.97 KMT2A (0.38) MEN1KMT2AAPEX1SMN1; SMN2ACHE
Bromide SCHEMBL27245942 0.97 BBOX1 (0.38) MEN1KMT2AAPEX1SMN1; SMN2ACHE
Hydrochloric Acid SCHEMBL7979134 0.95 APEX1 (0.41) MEN1KMT2AAPEX1SMN1; SMN2ACHE
Bromide SCHEMBL11035558 0.93 MEN1 (0.55) MEN1KMT2AAPEX1SMN1; SMN2ACHE
Bromide SCHEMBL5550538 0.91 DNM1 (0.50) KMT2ASMN1; SMN2HSD17B10TSHRDNM1
Bromide SCHEMBL3316250 0.91 DNM1 (0.50) KMT2ASMN1; SMN2HSD17B10TSHRDNM1
Bromide SCHEMBL22159436 0.91 DNM1 (0.50) KMT2ASMN1; SMN2HSD17B10TSHRDNM1
Bromide SCHEMBL11169923 0.91 DNM1 (0.50) KMT2ASMN1; SMN2HSD17B10TSHRDNM1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7125547-B2 Poly(diallylamine)-based bile acid sequestrants GENZYME CORPORATION (US) 2006-10-24 US claimed
US-20040151687-A1 Poly(diallylamine)-based bile acid sequestrants GENZYME CORPORATION 2004-08-05 US claimed
US-6726905-B1 LOWERING SERUM PHOSPHATE GENZYME CORPORATION 2004-04-27 US claimed
US-6610283-B1 Method for removing bile acids from a patient and certain polymers of use in the method. The method comprises the step of administering to the patient a therapeutically effective amount of a polymer composition which includes a a GENZYME CORPORATION 2003-08-26 US claimed
US-6203785-B1 ADMINISTERING CROSSLINKED CATIONIC POLYMER ANTICHOLESTEROL AGENTS GELTEX PHARMACEUTICALS, INC. 2001-03-20 US claimed
WO-1999022743-A1 POLY(DIALLYLAMINE)-BASED PHOSPHATE BINDERS GELTEX PHARMACEUTICALS, INC. (US) 1999-05-14 WO claimed
US-20070190021-A1 Poly(diallylamine)-based bile acid sequestrants HOLMES-FARLEY STEPHEN R 2007-08-16 US disclosed
US-7125547-B2 Poly(diallylamine)-based bile acid sequestrants GENZYME CORPORATION (US) 2006-10-24 US disclosed
US-20040151687-A1 Poly(diallylamine)-based bile acid sequestrants GENZYME CORPORATION 2004-08-05 US disclosed
US-6726905-B1 LOWERING SERUM PHOSPHATE GENZYME CORPORATION 2004-04-27 US disclosed
US-6692732-B2 Administering cationic polymers to mammals to prevent poisons or antigens from microorganisms such as bacteria, viruses, fungi or parasites; deactivation GENZYME CORPORATION 2004-02-17 US disclosed
US-20040009145-A1 IONIC POLYMERS AS TOXIN-BINDING AGENTS GELTEX PHARMACEUTICALS, INC. 2004-01-15 US disclosed
US-6610283-B1 Method for removing bile acids from a patient and certain polymers of use in the method. The method comprises the step of administering to the patient a therapeutically effective amount of a polymer composition which includes a a GENZYME CORPORATION 2003-08-26 US disclosed
US-20020114774-A1 Ionic polymers as toxin-binding agents GELTEX PHARMACEUTICALS, INC. 2002-08-22 US disclosed
US-6290947-B1 IN ONE EMBODIMENT, THE POLYMER IS A COPOLYMER COMPRISING A MONOMER HAVING A PENDANT AMMONIUM GROUP AND A HYDROPHOBIC MONOMER. GELTEX PHARMACEUTICALS, INC. 2001-09-18 US disclosed
US-6203785-B1 ADMINISTERING CROSSLINKED CATIONIC POLYMER ANTICHOLESTEROL AGENTS GELTEX PHARMACEUTICALS, INC. 2001-03-20 US disclosed
WO-1999022743-A1 POLY(DIALLYLAMINE)-BASED PHOSPHATE BINDERS GELTEX PHARMACEUTICALS, INC. (US) 1999-05-14 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070190021-A1 Poly(diallylamine)-based bile acid sequestrants NR1H4, SLC10A2, SLC10A1 ACHE 4819/4885MEN1 3103/4885KMT2A 3269/4885
US-20040151687-A1 Poly(diallylamine)-based bile acid sequestrants NR1H4, SLC10A2, SLC10A1 ACHE 4834/4885MEN1 3831/4885KMT2A 2729/4885
US-20020114774-A1 Ionic polymers as toxin-binding agents PIGS, ANTXR2, MSN ACHE 1151/4885MEN1 1450/4885KMT2A 3812/4885
US-20040009145-A1 IONIC POLYMERS AS TOXIN-BINDING AGENTS PIGS, ANTXR2, MSN ACHE 1151/4885MEN1 1450/4885KMT2A 3812/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.